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核苷酸与硅胶表面壳聚糖层的相互作用:在分子水平上建立作用机制。

Nucleotide Interaction with a Chitosan Layer on a Silica Surface: Establishing the Mechanism at the Molecular Level.

机构信息

Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16 C, 106 91 Stockholm, Sweden.

Chuiko Institute of Surface Chemistry of National Academy of Sciences of Ukraine, 17 General Naumov Street, 03164 Kyiv, Ukraine.

出版信息

Langmuir. 2021 Feb 2;37(4):1511-1520. doi: 10.1021/acs.langmuir.0c03050. Epub 2021 Jan 15.

Abstract

The growing interest in gene therapy is coupled with the strong need for the development of safe and efficient gene transfection vectors. A composite based on chitosan and fumed silica has been found to be a prospective gene delivery carrier. This study presents an investigation of the nature of the bonds between a series of nucleotides with a chitosan layer deposited on a fumed silica surface. Experimentally measured surface complex formation constants (log) of the nucleotides were found to be in the range of 2.69-4.02, which is higher than that for the orthophosphate (2.39). Theoretically calculated nucleotide complexation energies for chitosan deposited on the surface range from 11.5 to 23.0 kcal·mol, in agreement with experimental data. The adsorption of nucleotides was interpreted using their calculated speciation in an aqueous solution. Based on the structures of all optimized complexes determined from quantum-chemical PM6 calculations, electrostatic interactions between the surface-located NH groups and -POH-/-PO fragments of the nucleotides were identified to play the decisive role in the adsorption mechanism. The saccharide fragment of monophosphates also plays an important role in the binding of the nucleotides to chitosan through the creation of hydrogen bonds.

摘要

人们对基因治疗的兴趣日益浓厚,同时也强烈需要开发安全、高效的基因转染载体。基于壳聚糖和气相二氧化硅的复合材料已被发现是一种有前途的基因传递载体。本研究探讨了一系列核苷酸与沉积在气相二氧化硅表面的壳聚糖层之间的键合性质。实验测量的表面配合物形成常数(log)核苷酸的范围为 2.69-4.02,高于正磷酸盐(2.39)。理论计算的沉积在表面上的壳聚糖的核苷酸络合能范围为 11.5 至 23.0 kcal·mol,与实验数据一致。通过计算它们在水溶液中的形态来解释核苷酸的吸附。基于从量子化学 PM6 计算中确定的所有优化配合物的结构,确定表面定位的 NH 基团和核苷酸的 -POH/-PO 片段之间的静电相互作用在吸附机制中起决定性作用。单磷酸盐的糖片段也通过氢键的形成在核苷酸与壳聚糖的结合中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c18d/7880576/42de32f531be/la0c03050_0002.jpg

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